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苯二氮䓬类药物的药效学:生物相速率限制机制的证据。

Benzodiazepine pharmacodynamics: evidence for biophase rate limiting mechanisms.

作者信息

Ellinwood E H, Nikaido A M, Heatherly D G, Bjornsson T D

出版信息

Psychopharmacology (Berl). 1987;91(2):168-74. doi: 10.1007/BF00217057.

Abstract

Pharmacokinetics do not adequately reflect recovery from cognitive neuromotor impairment induced by most benzodiazepines. This paper examines across time the nature of the relationship of effect to serum concentration of three benzodiazepines. Using the same protocol lorazepam, alprazolam, diazepam and placebo were administered to eight healthy males at doses of 0.057, 0.029, 0.286 and 0.000 mg/kg, body weight, respectively for the first study and at 0.028, 0.014, 0.143 and 0.000 mg/kg, respectively, for the second study. After each dose administration multiple measurements were made over a period of 5.5-11.5 h using two different psychomotor performance tests. Serum drug concentrations were also measured. The profiles for diazepam and alprazolam effects demonstrate a stepwise decrement in the slopes of the concentration versus response curves across time, illustrating the rapid development of acute tolerance. In contrast, lorazepam induced a remarkably constant relationship between concentration and effect across testing intervals.

摘要

药代动力学不能充分反映大多数苯二氮䓬类药物所致认知神经运动功能损害的恢复情况。本文对三种苯二氮䓬类药物效应与血清浓度之间关系的性质进行了长期研究。在第一项研究中,按照相同方案分别向8名健康男性受试者给予氯硝西泮、阿普唑仑、地西泮和安慰剂,剂量分别为0.057、0.029、0.286和0.000 mg/kg体重;在第二项研究中,剂量分别为0.028、0.014、0.143和0.000 mg/kg体重。每次给药后,使用两种不同的精神运动性能测试,在5.5 - 11.5小时内进行多次测量。同时测量血清药物浓度。地西泮和阿普唑仑效应的曲线显示,随着时间推移,浓度 - 反应曲线的斜率呈逐步下降趋势,表明急性耐受性迅速形成。相比之下,氯硝西泮在整个测试期间诱导的浓度与效应之间的关系非常稳定。

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